HRID1865558

反应详情

EQUATION

反应方程式

HRID 1865558 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
0 °C

PROCEDURE

实验过程

methyl 4-(2-bromoacetyl)phenylcarbamate: 4-Aminoacetophenone was suspended in a 1:1 mixture of dioxane and water (150 mL), and NaOH (4.4 g, 0.11 mol) was added. The mixture was stirred until the NaOH dissolved, then cooled to 0° C. prior to dropwise addition of methylchloroformate (8.5 mL, 0.11 mol). The resulting mixture was stirred at 0° C. for an additional 10 min then at rt for 2 h, followed by standing overnight. The solvent was removed by evaporation and the residual solids were partitioned between EtOAc and water. The layers were separated and the aqueous was reextracted 2× with EtOAc. The combined organic extracts were dried over MgSO4, filtered and evaporated to yield a tan powder. The crude product was suspended in EtOAc, washed 3× with 1N HCl to remove unreacted aniline, then washed with brine, dried over MgSO4, filtered and evaporated to provide methyl-4-acetylphenylcarbamate as an orange/tan solid (11.2 g, 53%). A portion of this material (3 g, 15.53 mmol) was suspended in CHCl3 (60 mL) and bromine (0.960 mL, 18.63 mmol) was added in small portions. About halfway through the addition, most of the starting material had dissolved in the dark orange reaction mixture. At this point, the mixture quickly decolorized with the formation of a tan precipitate. The remaining bromine was added over ˜5 min, then the mixture was stirred at rt. After ˜30 min, the solid product was collected by filtration and washed with CHCl3 and air-dried overnight to provide the bromoketone (3.25 g, 77%) which was used without further purification. 1HNMR (500 MHz, DMSO-d6) δ: 10.14 (1H, s), 7.95 (2H, d, J=8.8 Hz), 7.59 (2H, d, J=8.8 Hz), 4.83 (2H, s), 3.57-3.83 (3H, m).

WORKUP

后处理

  1. additionwas added
  2. dissolutiondissolved
  3. waitat rt for 2 h
  4. waitby standing overnight
  5. customThe solvent was removed by evaporation
  6. customthe residual solids were partitioned between EtOAc and water
  7. customThe layers were separated
  8. dry with materialThe combined organic extracts were dried over MgSO4
  9. filtrationfiltered
  10. customevaporated
  11. customto yield a tan powder
  12. washwashed 3× with 1N HCl
  13. customto remove unreacted aniline
  14. washwashed with brine
  15. dry with materialdried over MgSO4
  16. filtrationfiltered
  17. customevaporated